Quality & Compliance Lead - Mexico & Northern Cluster

Johnson & Johnson MedTech; Ciudad de México; Presencial; MXN 600.000 - 900.000; Jornada completa

Descripción de la vacante

Johnson & Johnson’s DePuy Synthes is seeking a Quality Affairs professional to ensure products, processes, and services meet regulatory requirements and quality standards while supporting patient safety and business performance. This role partners with manufacturing, regulatory, and quality teams to drive continuous improvement across functions.

The position requires a life sciences or related degree, 2–4 years of relevant experience, and English proficiency; travel may be necessary as the

Formación

• Experience working in a regulated quality, compliance, regulatory affairs, or medical device environment.
• Knowledge of quality systems, documentation controls, and compliance processes.
• Ability to review quality records, audit findings, and inspection outcomes and support corrective actions.
• Strong analytical, organizational, and problem-solving skills.
• Experience using Microsoft Office applications and quality-related systems.
• Generally requires 2–4 years of relevant work experience.

Responsabilidades

• Support the execution and maintenance of Quality Management System (QMS) processes and related documentation.
• Coordinate quality and compliance activities to ensure alignment with internal procedures and applicable regulatory requirements.
• Assist with internal and external audits, inspections, and compliance assessments.
• Review, maintain, and control quality documentation, records, procedures, and training materials.
• Support investigations, corrective and preventive actions (CAPA), and continuous improvement initiatives.
• Analyze quality metrics, trends, and performance indicators and prepare reports for stakeholders.
• Collaborate with cross-functional teams to ensure quality standards are understood, implemented, and maintained across operations
• Maintain accurate records and support readiness for regulatory submissions, inspections, and audits.
• Research changes in regulatory requirements and industry standards and support implementation activities.
• Promote a culture of compliance, continuous improvement, and patient-focused quality.

Conocimientos

Quality Systems

ISO 9001

CAPA

Audit experience

Regulatory knowledge

Educación

Bachelor’s degree

Advanced degree

Descripción del empleo

Johnson & Johnson’s DePuy Synthes is seeking a Quality Affairs professional to ensure products, processes, and services meet regulatory requirements and quality standards while supporting patient safety and business performance. This role partners with manufacturing, regulatory, and quality teams to drive continuous improvement across functions.

The position requires a life sciences or related degree, 2–4 years of relevant experience, and English proficiency; travel may be necessary as the